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Abraham Flexner on staff at the
Carnegie
Foundation, and funded by the Rockefeller Foundation, 'sourced'
the American 'medical' reformation following US Congressional acceptance of the
"Flexner
Report."
This infamous treatise exclusively benefited the IG Farben/Rockefeller
petrochemical pharmaceutical alliance that vilified every form of natural
healing, replacing nutrition with
petrochemicals to monopolize
healthcare.
In her 1993 book The Molecular Vision of Life,
Dr. Lily E. Kay, whom a 2001 MIT News Office obituary referred to as "one of
the outstanding historians of biology of her generation," argued that the "new
biology" was largely forged by the Rockefeller
Foundation and its subsidiary program at the
California Institute of
Technology (Caltech) through a consensus between a scientific elite and
a business elite whose broader aims centered on eugenics and the need to create
a mechanism of social control and human engineering:
"The new science
did not just evolve by natural
selection of randomly distributed disciplinary variants, nor did it ascend
solely through the compelling power of its ideas and its leaders. Rather, the
rise of the new biology was an expression
of the systematic cooperative efforts of America's scientific establishment
- scientists and their patrons - to direct
the study of animate phenomena
along selected paths toward a shared vision of science and society." - Dr. Lily
E. Kay
Practioners of
alternative healing methods consider the application of chemical toxins and
surgeries to be 'allopathic medicine'.
"The Allopathic approach to
healing is a far cry from Hippocratic method of healing which attempted to use
natural methods of balancing 'humors.'
"The term "allopathy" was
invented by German physician Samuel Hahnemann.
He conjoined allos
"opposite" and pathos "suffering" as a referent to harsh medical practices of
his era which included bleeding, purging, vomiting and
the administration of
highly toxic drugs.
These practices were based on the ancient Greek
humoral theory which attributed disease to an imbalance of four humors (i.e.,
blood, phlegm, and black and yellow bile) and
four bodily conditions (i.e, hot, cold,
wet and dry) that corresponded to
four elements (earth,
air, fire, and water).
Physicians following the Hippocratic tradition attempted to balance the
humors by treating symptoms with "opposites." - William
Jarvis
Reliance on toxic chemical drugs is based
upon the philosophy of Santorio Santorio, also known as
Sanctorius.
Santorio
argued throughout his career that the fundamental properties of human health
were mathematical ones,
such as number, position, and form - breaking from describing the body and its
functions in terms of Aristotelian (and Galenic) elements and qualities.
This radical break with traditional medical theory and natural
philosophy proposed the human body was a machine the workings of which were
determined by the shapes and positions of its interlocking parts that could be
broken down into constituent molecules.
Beginning from a fundamentally
unsound foundation Santorio made 'phenomenal' properties, seen from
a mechanistic Newtonian viewpoint,
central to his worldview of
nature and
medicine.
While the central
metaphor of Aristotelian natural philosophy and Galenic medicine was organic,
Santorio made it mechanical: the
clock (more generally,
the machine) became the
metaphor for nature opening up a window for
biochemistry and, later,
molecular biology.
While his 'trail and error' experiments were
replicated and augmented by his followers and finally surpassed by those of
Antoine Lavoisier he is still regarded by many as the father of
experimental
physiology.
“The pen is mightier than the sword.
Mightier than either the pen or the sword is the pill.”
Aldous
Huxley
"How does a physician subscribing to "first do no harm" find himself or herself
prescribing either drugs that are inherently harmful or drugs at hazardous
levels? Follow the money". - Tom Pula
"When patients ask for a drug, they tend to get the
drug regardless of whether it is appropriate for them." -
Joel Weissman, health policy expert
"According to the 2005 Partnership Attitude
Tracking Study, 40% believe that prescription medicines are
"much safer" to use than
illegal drugs.
These controlled substances are not just highly
dangerous, but they can prove lethal." -
Joseph T. Rannazzisi, May 16, 2007
1990 Americans spend $40 billion on
prescription
medications.
1998 JAMA study estimates 106,000
prescription
medications deaths.
2004
Americans spend $190 billion on prescribed
medications.
2006 Americans spend $280
billion on prescription
medication.
2009 Pharmaceutical manufacturers gain
FDA approval to distribute medical journal articles describing unapproved
off-label uses of drugs.
2011 Record 4 billion prescriptions in US
2015 Americans spend $413 billion on prescribed
drugs.
Over 1000% increase in twenty five
years.
80% of the active
pharmaceutical ingredients used to make drugs sold in America are imported and
40% of finished drugs are made in
foreign countries - much of both from China.
When making a
solution, the manufacturer must first decide what degree of chemical purity is
needed based on the intended use.
The following list describes the
seven most common grades for chemicals and reagents, from highest to lowest
grade/purity:
ACS grade meets or exceeds purity standards set by the
American Chemical Society (ACS). This grade is acceptable for food, drug, or
medicinal use and can be used for ACS applications or for general procedures
that require stringent quality specifications and a purity of =95%.
Reagent grade is generally equal to ACS grade (=95%) and is acceptable
for food, drug, or medicinal use and is suitable for use in many laboratory and
analytical applications.
USP grade meets or exceeds requirements of the
United States Pharmacopeia (USP). This grade is acceptable for food, drug, or
medicinal use.
United States Pharmacopeia is acceptable for most
laboratory purposes, but formulation should always be reviewed to ensure
appropriate methodology.
NF grade meets or exceeds requirements of the
National Formulary (NF).
The USP and the NF (USP– NF) jointly publish
a book of public pharmacopeial standards for chemical and biological drug
substances, dosage forms, excipients, compounded preparations, medical devices,
and dietary supplements.
Laboratory grade is the most popular grade for
use in educational applications, but its exact levels of impurities are
unknown. While excellent for teaching and training, it is not pure enough to be
offered for food, drug, or medicinal use.
Purified grade, also called
pure or practical grade, meets no official standard; it is not pure enough to
be offered for food, drug or medicinal use of any kind.
Technical grade
is used for commercial and industrial purposes; it is not pure enough to be
offered for food, drug or medicinal use of any kind.
Of critical
importance here is the allowance of a huge amount of contaminants.
Purity of 95% with an allowance of 5% contaminants may not matter in a
variety of applications but is critical in food, drug or medicinal use of any
kind.
No manufacturer would dare to use a lower quality to increase
profit !
No lab technicians would 'accidentally' use a lower quality
grade!
"Apothecary, n.
The physicians's accomplice,
undertaker's benefactor and grave worm's provider."
Ambrose Bierce
The
US Chamber of Commerce
and the Pharmaceutical Research and Manufacturers of America ("PHRMA")
argue that exposing generic pharmaceutical manufacturers to state law tort
liability will negatively impact the American healthcare system by denying
physicians and patients in some states access to certain generic medications.
Under the Supremacy Clause of the US Constitution, federal laws
represent the supreme law of the land and
may preempt or override state laws.
1984 Hatch-Waxman Act
allows generic drug makers to bypass testing requirements and enter the market
if they can prove that their generic drug is equivalent to
an approved brand-name drug
and carries the same labeling.
1992
Prescription Drug User Fee Act (PDUFA) is marketed for its
miraculous ability to reduce the time and cost of bringing lifesaving drugs to
market in time to save substantial numbers of 'disease' victims.
(Choose two or more of the above to comply with
Obamacare.)
If the FDA rules a drug is safe,
even if it
kills a loved one,
(or a loved one kills you !)
you have no recourse !
"Sick days are typically unplanned, which results
in significant burdens to corporations ." - Rick Chaifetz, CEO of ComPysch
"People are being forced to chose between being
a good employee or being
a good family member" - Linda Meric,
director of 9 to 5, National Association of Working Women
June 23, 2011 PLIVA, Inc. v.
Mensing
Federal drug regulations applicable to generic drug
manufacturers directly conflict
with, and thus preempt, state-law tort claims alleging a failure to provide
adequate warning labels.
Supreme Court holds
"sameness" requirement of Hatch-Waxman Act preempts state imposition of
stricter labeling requirements on generic drugs.
Supreme Court rules
that federal law related to pharmaceutical regulations preempts a person's
ability to sue in state courts and allege that a generic drug is poorly
designed and manufactured.
Supreme Court rules that
the FDA has authority over
pharmaceuticals.
80% of all drugs consumed in the US are now
exempt from liability for
side effects, mislabeling and
virtually any other adverse reactions.
Generic pharmaceutical
manufatures become exempt from multi-million dollar court-imposed settlements
and no longer have to worry about safety or side effects, they awarded to
victims of their generic drugs.
"Today's court decision provides
a disincentive for generic
makers of drugs to monitor safety of their products and to make sure that
they have a surveillance system in place to detect adverse events that pose a
threat to patients." - Michael Carome, Public Citizen's Health Research
Group
June 24, 2013 Mutual Pharmaceutical Co. v.
Bartlett
Generic drug manufactures cannot be held liable
under state law for not adequately labeling medication when federal law
prohibits them from changing the label from the original brand name
drug.
Commercial messages are ingrained by
endlessly repetition.
Human aspire to be elevated
into a position outside of nature.
But many commonly prescribed
pharmaceuticals promote cancer !
Hormone replacement therapy is among the
most controversial medications.
Industrially produced
estrogen can promote uterine as
well as breast
cancer.
"Taking menopause hormones for five years doubles the risk
for breast cancer." -
Marilynn Marchione 12/13/08
Many pharmaceuticals have warnings about
cancer creation.
Omeprazole
(Prilosec©) causes abnormal
cell growth and stomach tumors (carcinoids) in rats.
Spironolactone
(Aldactazide©, Aldactone©) a
blood pressure medicine,
sometimes prescribed for hormonal imbalances and facial hair growth in women,
causes tumors in rats.
Elidel© and Protopic©, are associated with lymphoma and
skin cancer.
The rheumatoid
arthritis injections Cimzia©, Enbrel©, Humira© and
Remicade©, expensive bio-tech drugs have been associated with
lymphoma.
"In the New
England Journal of Medicine, Sept. 25,
2008, investigators noted a
higher incidence of cancer in subjects taking
Vytorin©." - Joe
Graedon, pharmacologist & Teresa Graedon, nutrition expert
"Today's
announcement that the ENHANCE study failed to find any positive benefit from
the addition of Zetia® to a common, inexpensive, generic therapy raised
concerns that attempts were made to mask the minimal value of this new drug."-
Representative John Dingell, Committee on Energy and Commerce chairman
1/15/08
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forged a populace unable to discern
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